The HUWE1 gene mental retardation X-linked syndromic Turner type genetic test is a specialized diagnostic assessment conducted to identify mutations in the HUWE1 gene, which are associated with a form of X-linked mental retardation known as Turner syndrome. This condition, not to be confused with Turner syndrome that affects females due to an X chromosome abnormality, is a different entity and involves intellectual disability, developmental delays, and sometimes physical abnormalities. The test is crucial for families seeking to understand the genetic underpinnings of intellectual and developmental challenges in males, providing essential information for managing and supporting affected individuals.
Performed at DNA Labs UAE, a leading facility in genetic testing and analysis, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing the genetic material for specific mutations in the HUWE1 gene. This gene plays a vital role in the regulation of DNA damage response and cell cycle control, and mutations can lead to neurological and developmental disorders.
The cost of the HUWE1 gene mental retardation X-linked syndromic Turner type genetic test at DNA Labs UAE is 4400 AED. This cost reflects the sophisticated technology and expertise required to accurately identify mutations in the HUWE1 gene. For families and individuals considering this test, it represents a significant investment in understanding the genetic factors contributing to the condition, potentially leading to more personalized and effective management strategies.
The IQSEC2 gene mental retardation X-linked type 1 genetic test is a specialized diagnostic procedure designed to identify mutations in the IQSEC2 gene, which is located on the X chromosome. This gene plays a crucial role in cognitive development and functioning. Mutations in the IQSEC2 gene are associated with a form of intellectual disability known as X-linked mental retardation type 1. This condition primarily affects males and is characterized by varying degrees of cognitive impairment, learning disabilities, and sometimes behavioral problems.
The test is conducted through a blood sample, where DNA is extracted and analyzed for any genetic anomalies present in the IQSEC2 gene. It is particularly recommended for families with a history of X-linked intellectual disability or for individuals showing symptoms related to cognitive developmental delays without a known cause.
Conducted at DNA Labs UAE, a facility known for its advanced genetic testing services, the IQSEC2 gene test is available for a cost of 4400 AED. This test not only aids in the diagnosis of X-linked intellectual disability but also helps in understanding the condition better, guiding treatment plans, and providing information important for family planning.
The MID2 Gene Mental Retardation X-Linked Type 101 Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the MID2 gene, which are linked to a form of intellectual disability known as X-Linked Mental Retardation Type 101. This condition primarily affects males and is characterized by various degrees of cognitive impairment, developmental delays, and sometimes physical anomalies. The MID2 gene plays a crucial role in the development and function of the nervous system, and mutations in this gene can lead to the aforementioned intellectual disabilities.
The test is conducted through a detailed analysis of the patient's DNA, which is extracted from a blood sample. State-of-the-art genetic sequencing technologies are employed to identify any alterations in the MID2 gene that are associated with the condition. This test is crucial for families seeking to understand the genetic basis of intellectual disabilities in their members, as it can provide definitive answers and guide towards appropriate management and therapy options.
The MID2 Gene Mental Retardation X-Linked Type 101 Genetic Test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED, reflecting the comprehensive nature of the analysis and the specialized expertise required to interpret the results. DNA Labs UAE is equipped with the latest in genetic testing technology and staffed by experts in the field, ensuring that patients receive accurate and actionable information about their genetic health.
The DDX3X Gene Mental Retardation X-Linked Type 102 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the DDX3X gene, which have been associated with X-linked mental retardation type 102. This condition, primarily affecting neurological development, can lead to a range of cognitive impairments and developmental delays, with symptoms and severity varying widely among individuals. The test involves analyzing the patient's DNA to detect any abnormalities or mutations in the DDX3X gene that could be responsible for the condition.
Performed at DNA Labs UAE, a leading facility in genetic diagnostics, this test offers families and individuals crucial information regarding the genetic underpinnings of mental retardation and related developmental issues. The cost of the test is set at 4400 AED, reflecting the advanced technology and expertise required to accurately identify mutations in the DDX3X gene. By opting for this test, patients gain access to critical insights that can guide treatment decisions, inform about potential developmental expectations, and offer a clearer understanding of the genetic factors contributing to the condition.
The MECP2 Gene Mental Retardation X-Linked Type 13 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the MECP2 gene, which are closely associated with X-linked mental retardation type 13. This condition is part of a spectrum of neurological disorders that can affect cognitive function, development, speech, and motor skills, often manifesting early in life. The MECP2 gene plays a crucial role in the development of the nervous system and its proper functioning. Mutations in this gene can lead to various degrees of intellectual disability and physical challenges.
Given the complexity of the genetic analysis, the test is priced at 4400 AED. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the state-of-the-art facilities of DNA Labs UAE. The laboratory employs cutting-edge genetic sequencing technologies to detect any abnormalities in the MECP2 gene that might indicate the presence of X-linked mental retardation type 13.
This test is particularly recommended for families with a history of the condition or when children present with symptoms that could suggest a genetic disorder affecting cognitive and physical development. Early diagnosis through the MECP2 Gene Mental Retardation X-Linked Type 13 Genetic Test can be crucial in managing the condition, allowing for tailored interventions and support to improve the quality of life for those affected.
The UPF3B Gene Mental Retardation X-Linked Type 14 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the UPF3B gene, which is located on the X chromosome. This gene plays a critical role in the nonsense-mediated mRNA decay pathway, which is essential for normal brain development and function. Mutations in the UPF3B gene have been linked to various neurodevelopmental disorders, including intellectual disability, autism spectrum disorders, and schizophrenia. These conditions are often referred to collectively as X-linked mental retardation type 14.
The test is particularly valuable for families with a history of X-linked intellectual disabilities, providing crucial information for genetic counseling, early intervention, and personalized management plans for affected individuals. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific mutations in the UPF3B gene.
The cost of the UPF3B Gene Mental Retardation X-Linked Type 14 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expert analysis required to accurately identify mutations in the UPF3B gene. Patients considering this test are advised to consult with a genetic counselor or healthcare provider to understand the implications of the results and the best course of action based on the findings.
The CUL4B gene mental retardation X-linked type 15 genetic test is a specialized diagnostic tool designed to identify mutations in the CUL4B gene, which are implicated in a form of X-linked mental retardation (XLMR). This condition, also known as Cabezas syndrome, is characterized by various intellectual disabilities, physical anomalies, and sometimes behavioral issues. The test is crucial for families with a history of XLMR, as it aids in the early diagnosis and management of the condition.
Conducted at DNA Labs UAE, a leading facility in genetic testing, this test involves analyzing the patient's DNA to detect abnormalities in the CUL4B gene. The process is meticulous and requires a sample of the patient's blood or saliva. DNA Labs UAE employs state-of-the-art technology and follows stringent protocols to ensure accurate and reliable results.
The cost of the CUL4B gene mental retardation X-linked type 15 genetic test is 4400 AED. While the price may seem steep, it is a valuable investment in understanding and potentially mitigating the impact of this genetic condition. Early diagnosis can lead to better management of symptoms, tailored educational strategies, and improved overall quality of life for affected individuals.
The FGD1 Gene Mental Retardation X-Linked Type 16 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the FGD1 gene, which are associated with X-linked mental retardation type 16 (MRX16). This condition is a rare genetic disorder that affects cognitive function and can lead to various degrees of intellectual disability. The test aims to provide crucial information for the accurate diagnosis and management of individuals suspected to have MRX16, enabling targeted interventions and support.
Carried out through advanced genetic sequencing techniques, the test analyzes the FGD1 gene for specific mutations that are known to cause the disorder. This is particularly important for families with a history of the condition, as it can help in understanding the risk for future generations.
The cost of the FGD1 Gene Mental Retardation X-Linked Type 16 Genetic Test at DNA Labs UAE is 4400 AED. The investment in this test can be invaluable for affected families, offering them insights into the genetic underpinnings of the condition and guiding them towards appropriate medical and psychological support services. It's a critical step in the journey towards personalized medicine, where treatments and interventions can be tailored to the individual based on their unique genetic makeup.
The KAT6A Gene Mental Retardation Autosomal Dominant Type 32 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the KAT6A gene that are associated with Autosomal Dominant Mental Retardation Type 32. This condition is characterized by intellectual disability and possibly other neurological or physical abnormalities, resulting from genetic variations that affect normal brain development and function. The test, priced at 4400 AED, involves analyzing the patient's DNA to detect specific genetic alterations in the KAT6A gene that are known to cause this disorder. By identifying these mutations, the test provides essential information for accurate diagnosis, which is crucial for management, treatment planning, and genetic counseling for affected individuals and their families.
The "POGZ Gene Mental Retardation Autosomal Dominant Type 37 Genetic Test" is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the POGZ gene, which have been associated with autosomal dominant mental retardation type 37 (MRD37). This condition is characterized by various neurological and developmental challenges, including intellectual disability, delayed speech and motor milestones, and sometimes physical abnormalities. The test, priced at 4400 AED, involves analyzing the patient's DNA to detect alterations in the POGZ gene that could lead to the development of MRD37, providing crucial information for the diagnosis, management, and understanding of the condition. By pinpointing specific genetic mutations, this test enables tailored care and support strategies for affected individuals and their families.
